Nimodipine
CAS No. 66085-59-4
Nimodipine( Admon | BAY-e 9736 | Periplum )
Catalog No. M15515 CAS No. 66085-59-4
Nimodipine(Nimotop) is a dihydropyridine derivative and an analogue of the calcium channel blocker nifedipine, with antihypertensive activity.Nimodipine decreases intracellular free Ca2+,Beclin-1 and autophagy.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 36 | In Stock |
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| 100MG | 43 | In Stock |
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| 500MG | 65 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameNimodipine
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NoteResearch use only, not for human use.
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Brief DescriptionNimodipine(Nimotop) is a dihydropyridine derivative and an analogue of the calcium channel blocker nifedipine, with antihypertensive activity.Nimodipine decreases intracellular free Ca2+,Beclin-1 and autophagy.
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DescriptionNimodipine(Nimotop) is a dihydropyridine derivative and an analogue of the calcium channel blocker nifedipine, with antihypertensive activity.Nimodipine decreases intracellular free Ca2+,Beclin-1 and autophagy.(In Vitro):Nimodipine (1.5~150 μg/ml; 15 minutes; B16a and W256 cells) results in a dose-dependent inhibition of B16a and W256 tumor-cell-induced platelet aggregation. Nimodipine is also inhibitory in a homologous system.(In Vivo):Nimodipine (0.2 μg/μl, intrathecal administration) prevents subarachnoid hemorrhage-associated cerebral vasospasm by prophylactic continuous intrathecal administration.Nimodipine(0.1~80 mg/kg; p.o.) results in a significant dose-dependent inhibition of spontaneous metastasis.
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In VitroNimodipine (1.5~150 μg/ml; 15 minutes; B16a and W256 cells) results in a dose-dependent inhibition of B16a and W256 tumor-cell-induced platelet aggregation. Nimodipine is also inhibitory in a homologous system.
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In VivoNimodipine (0.2 μg/μl, intrathecal administration) prevents subarachnoid hemorrhage-associated cerebral vasospasm by prophylactic continuous intrathecal administration.Nimodipine(0.1~80 mg/kg; p.o.) results in a significant dose-dependent inhibition of spontaneous metastasis. Animal Model:New Zealand white rabbits Dosage:0.2 μg/μl Administration:Intrathecal administration Result:Prevented subarachnoid hemorrhage-associated cerebral vasospasm by prophylactic continuous intrathecal administration.
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SynonymsAdmon | BAY-e 9736 | Periplum
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PathwayEndocrinology/Hormones
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TargetAhR
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RecptorAhR| Calcium Channel| Mineralocorticoid Receptor
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number66085-59-4
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Formula Weight418.44
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Molecular FormulaC21H26N2O7
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Purity>98% (HPLC)
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SolubilityEthanol: 84 mg/mL (200.74 mM); DMSO: 84 mg/mL (200.74 mM)
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SMILESCC1=C(C(OCCOC)=O)C(C2=CC([N+]([O-])=O)=CC=C2)C(C(OC(C)C)=O)=C(C)N1
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Chemical Name3-isopropyl 5-(2-methoxyethyl) 2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Weant KA, et al. PharmacOthersapy. 2010 Apr;30(4):405-17.
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